FDA applicant

Nk Biotechnical Engineering Co.

Minneapolis, MN15 decisions1991–19940 recalls

FDA records 15 decisions for Nk Biotechnical Engineering Co. (Minneapolis, MN) from 1991 to 1994: 15 510(k) clearances. Most are in product codes LBB (Dynamometer, Ac-Powered) and KQX (Goniometer, Ac-Powered). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Nk Biotechnical Engineering Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nk Biotechnical Engineering Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nk Biotechnical Engineering Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Nk Biotechnical Engineering Co.

Which product codes does it file in?

What has FDA decided for it lately?